Our family’s Purple Heart Days serve as a powerful reminder that we are brave, strong, and ready to face any challenge head-on. On these days, we stand together, knowing that no one faces difficult moments alone. This tradition was inspired by two of our favorite books—The Kissing Hand by Audrey Penn and The Invisible String by Patrice Karst—as well as the memory of our beloved Aunty Patsy.
Years ago, during a particularly tough day, I placed a purple heart on Declan’s palm, as well as on my husband’s and mine, to remind us of our strength and connection. The purple heart became symbolic not only because of its meaning but also due to Aunt Patsy, who had recently gifted me a box of purple Sharpies, knowing it was my favorite color.
The purple heart now represents more than just that moment. It embodies our family’s resilience and love, as well as the valor symbolized by the military’s Purple Heart, given for courage and sacrifice. Just as every soldier has a unique story, our purple hearts remind us that we are not alone on our journey—each of us is walking our own path, but always with one another. We warmly invite and encourage everyone to join us on our journey, and in turn, we welcome the opportunity to walk alongside you on yours.
A purple heart is more than a symbol of sacrifice; it’s a testament to resilience. In the face of trials, it reminds us that true strength comes from standing tall, even when the world feels heavy.
Purple Heart Days have been a part of our family since 2016, but in 2023, we began documenting them as our community, both online and off, joined in. The strength of many purple hands coming together is truly inspiring. In October 2023, we faced the news that our middle son, Carter, needed a new pulmonary valve. His last open-heart surgery was at just 1 month old. Back then, our coping thought was, "He will never remember."
Now, at 7 years old, we knew he would remember this journey. What we wanted him to hold onto was the love and support surrounding him—and that’s exactly what happened. As we left the hospital, we had so much to celebrate. Thanks to the amazing traveling purple hearts throughout our community on the day of his second open heart surgery he will always remember being wrapped in the strenght of our incredible community.
This year, both Jolene and Declan faced medical challenges. Jolene received her third set of tubes, along with other treatments from the ORL department, to improve her hearing and reduce ear infections. We are also hopeful for Declan’s upcoming procedure to widen his sinus pathways, which should help reduce his winter illnesses and manage inflammation.
David Andrews
Hunter Henry
Kevin Pierce
Raheem Morris
We are truly blessed to live in an amazing town. The support we've received from GMES has been incredible, not just in academics but also in helping us navigate our children's medical and emotional needs. The staff and community there are the real A-listers in our lives, making a profound impact on our family's journey.
Know those moments when God puts you in the right place at the right time, that was tonight…Â
As most of you know Carter was diagnosed in utero with Tetralogy of Fallot. At the time of diagnosis the cardiologist shared with us that Shaun White the snowboarder also has TOF. In that moment the weight of the diagnosis seemed a little lighter. We weren’t sure if we were going to make this trip tonight but something in me told me to go (despite the insane weekend schedule we have.) There were tears, more hope for the future and a sense of celebration. Although, as much as Shaun has inspired us I told him that I needed to meet his mom. It is his mom I think of often as I watch Carter race up and down the soccer field or take the next level on the mountain. I remind myself that just as she didn’t hold Shaun back, I won’t hold Carter back—though sometimes, that’s easier said than done.
The moment doesn’t end there though. About two hours later as we were closing the place up a sweet couple comes up to us and said we over heard you tell someone your son has TOF and they proceed to tell us that they are expecting and just found out their baby was just diagnosed with TOF in utero. We shared with them the hurdles, the ups, the downs and the moments of amazingness. And wild the same amazing doctor will also be delivering their baby.
It was an all around powerful encounter filled with shared tears and hope—a connection we were meant to have, one that reminded us we’re all part of something bigger.